Frakefamide
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Systematic (IUPAC) name | |
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4-fluoro-L-phenylalanyl-N-[(2R)-2-(L-tyrosylamino)propanoyl]-L-phenylalaninamide
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Identifiers | |
CAS Number | 188196-22-7 |
ATC code | None |
PubChem | CID: 5493563 |
ChemSpider | 4591495 |
Chemical data | |
Formula | C30H34FN5O5 |
Molecular mass | 563.620 g/mol |
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Frakefamide (INN) is a synthetic, fluorinated opioid tetrapeptide with the amino acid sequence Tyr-D-Ala-(p-F)Phe-Phe-NH2 which acts as a peripherally-specific, selective μ-opioid receptor agonist.[1][2] Despite its inability to penetrate the blood-brain-barrier and enter the central nervous system,[1] frakefamide has potent analgesic effects and, unlike centrally-acting opioids like morphine, does not produce respiratory depression, indicating that its antinociceptive effects are mediated by peripheral μ-opioid receptors.[1][3] It was under development for the treatment of pain by AstraZeneca and Shire but was shelved after phase II clinical trials.[4][5]
See also
References
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- Drugs not assigned an ATC code
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- Analgesics
- Organofluorides
- Opioid peptides
- Peripherally selective drugs